HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440413Generated: October 27, 2026
Water → 4-(3,5-di-tertiary-butyl-4-hydroxy-N-methylanilino)benzoic acid
https://huagongshe.com/reaction/1440413
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-(3,5-Di-tertiary-butyl-4-hydroxyanilino)benzoic acid | HCID 13960406 | — |
| Solvent | Methyl iodide | HCID 6328 | — |
| Product | 4-(3,5-di-tertiary-butyl-4-hydroxy-N-methylanilino)benzoic acid | HCID 22401583 | — |
Reaction Steps
A solution of 3.4 g (0.010 mole) of 4-(3,5-di-tertiary-butyl-4-hydroxyanilino)benzoic acid (prepared in Example 1) in 35 ml of N,N-dimethylformamide and 3.5 ml of methyl iodide was heated at 95° C. for about 48 hours under nitrogen. The reaction mixture was poured into cold water and the resulting solid was collected and then taken up in chloroform. The chloroform solution was filtered, washed with water, dried with magnesium sulfate and evaporated to give a tan solid. This material was recrystallized first from benzene and then from a mixture of ethanol and water to give 1.5 g of white crystalline 4-(3,5-di-tertiary-butyl-4-hydroxy-N-methylanilino)benzoic acid, m.p. 240°-244° C. Analysis: Calculated for C22H29NO3 : % C, 74.3; % H, 8.2; % N, 3.9. Found: % C, 74.4; % H, 8.3; % N, 3.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05498745 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-78b02402a7e94c9ca1611ad64bb11f27 |
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| Source note | uspto-grants-1996_03 |
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